Associated Papers
A Novel Mutation of CADHERIN (CDH15) in an Iranian Boy With Borderline Intelligence Without Dysmorphism-A Case Report.
Ashrafi MR et al.
Clinical Case Reports, 2025
High-depth African genomes inform human migration and health.
Choudhury A et al.
Nature, 2020
33116287 (PubMed )
Supplement: 41586_2020_2859_MOESM3_ESM.xlsx › Supp_T19
Cadherins as targets for genetic diseases.
El-Amraoui A et al.
Cold Spring Harbor Perspectives in Biology, 2010
Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability.
Bhalla K et al.
American Journal of Human Genetics, 2008
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